Canonical Allele Identifier: CA658799770

Gene: AR

Linked Data

• ClinVar Variation Id: 504141
• ClinVar RCV Id: RCV000599127
• dbSNP Id: rs1555969382
• MyVariant Identifiers: chrX:g.66765008_66765126dup (hg19) ; chrX:g.67545166_67545284dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67545166_67545284dup , CM000685.2:g.67545166_67545284dup	GRCh38
NC_000023.10:g.66765008_66765126dup , CM000685.1:g.66765008_66765126dup	GRCh37
NC_000023.9:g.66681733_66681851dup	NCBI36
NG_009014.2:g.6135_6253dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.20_138dup	ENSP00000379358.4:p.Ala47TrpfsTer27
ENST00000374690.9:c.20_138dup MANE Select	ENSP00000363822.3:p.Ala47TrpfsTer27
ENST00000396044.8:c.20_138dup	ENSP00000379359.3:p.Ala47TrpfsTer27
ENST00000612452.5:c.20_138dup	ENSP00000484033.2:p.Ala47TrpfsTer27
ENST00000374690.7:c.20_138dup	ENSP00000363822.3:p.Ala47TrpfsTer27
ENST00000396044.7:c.20_138dup	ENSP00000379359.3:p.Ala47TrpfsTer27
ENST00000504326.5:c.20_138dup	ENSP00000421155.1:p.Ala47TrpfsTer27
ENST00000513847.5:n.347_465dup
ENST00000514029.5:c.20_138dup	ENSP00000425199.1:p.Ala47TrpfsTer27
ENST00000612010.4:c.20_138dup	ENSP00000482407.1:p.Ala47TrpfsTer27
ENST00000612452.4:c.-551_-433dup	ENSP00000484033.1:n.-551_-433dup
ENST00000613054.2:c.20_138dup	ENSP00000479013.1:p.Ala47TrpfsTer27
NM_000044.3:c.20_138dup	NP_000035.2:p.Ala47TrpfsTer27
NM_000044.4:c.20_138dup	NP_000035.2:p.Ala47TrpfsTer27
NM_001011645.3:c.-1764_-1646dup	NP_001011645.1:n.-1764_-1646dup
NM_001348061.1:c.20_138dup	NP_001334990.1:p.Ala47TrpfsTer27
NM_001348063.1:c.20_138dup	NP_001334992.1:p.Ala47TrpfsTer27
NM_001348064.1:c.20_138dup	NP_001334993.1:p.Ala47TrpfsTer27
NM_000044.6:c.20_138dup MANE Select	NP_000035.2:p.Ala47TrpfsTer27